MLH1 Rabbit mAb - A25641
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Catalog #
AB-A25641
Ab
135,00 €
The protein encoded by this gene can heterodimerize with mismatch repair endonuclease PMS2 to form MutL alpha, part of the DNA mismatch repair system. When MutL alpha is bound by MutS beta and some accessory proteins, the PMS2 subunit of MutL alpha introduces a single-strand break near DNA mismatches, providing an entry point for exonuclease degradation. The encoded protein is also involved in DNA damage signaling and can heterodimerize with DNA mismatch repair protein MLH3 to form MutL gamma, which is involved in meiosis. This gene was identified as a locus frequently mutated in hereditary nonpolyposis colon cancer (HNPCC).
Isotype | IgG |
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Datasheet URL | https://abclonal.com/instructions/pdf/A25641 |
Alternative Names | FCC2; COCA2; HNPCC; MLH-1; hMLH1; HNPCC2; LYNCH2; MMRCS1 |
Species | Human |
Source | Rabbit |
Purity | Affinity purification |
Immunogen | A synthetic peptide corresponding to a sequence within amino acids 350-450 of human MLH1 (NP_000240.1). |
Storage | Store at -20℃. Avoid freeze / thaw cycles.|Buffer: PBS with 0.05% proclin300,0.05% BSA,50% glycerol,pH7.3. |
Conjugate | Unconjugated |